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BDBM50124534 2-Methyl-1,2-dihydro-quinazolin-4-ylamine::2-methyl-1,2-dihydroquinazolin-4-amine::CHEMBL355856

SMILES: CC1Nc2ccccc2C(N)=N1

InChI Key: InChIKey=BFASSLCZFJPKRD-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50124534   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50124534
PNG
(2-Methyl-1,2-dihydro-quinazolin-4-ylamine | 2-meth...)
Show SMILES CC1Nc2ccccc2C(N)=N1 |c:11|
Show InChI InChI=1S/C9H11N3/c1-6-11-8-5-3-2-4-7(8)9(10)12-6/h2-6,11H,1H3,(H2,10,12)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 9.80E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of iNOS


J Med Chem 51: 2481-91 (2008)


Article DOI: 10.1021/jm701314u
BindingDB Entry DOI: 10.7270/Q2GX4CF5
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50124534
PNG
(2-Methyl-1,2-dihydro-quinazolin-4-ylamine | 2-meth...)
Show SMILES CC1Nc2ccccc2C(N)=N1 |c:11|
Show InChI InChI=1S/C9H11N3/c1-6-11-8-5-3-2-4-7(8)9(10)12-6/h2-6,11H,1H3,(H2,10,12)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 9.80E+3n/an/an/an/an/an/a



AstraZeneca R& D Charnwood

Curated by ChEMBL


Assay Description
Inhibitory activity of compound against human inducible nitiric oxide synthase


J Med Chem 46: 913-6 (2003)


Article DOI: 10.1021/jm0255926
BindingDB Entry DOI: 10.7270/Q2S75H3M
More data for this
Ligand-Target Pair